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arXiv:1708.00719 · Physical Review A

ac Stark effect in ultracold polar Rb87Cs133 molecules

Philip D. Gregory, Jacob A. Blackmore, J. Aldegunde, Jeremy M. Hutson, Simon L. Cornish

Published Aug 11, 2017• 35 citations
arXivHTMLPDF

Abstract

ac Stark shifts of ultracold polar RbCs molecules are measured with hyperfine resolution. Due to coupling from the anisotropic component of the polarizability, the hyperfine levels of the first excited rotational state show an intricate pattern of avoided crossings as a function of laser intensity.
DOI
10.1103/physreva.96.021402

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Effects of static electric and magnetic fields on the differential ac Stark shifts for microwave transitions in ultracold bosonic 87{}^{87}87Rb133{}^{133}133Cs molecules are studied experimentally. The ac Stark effect is greatly simplified by applying a dc electric field in addition to the magnetic field.
This thesis presents the development of a toolbox for the coherent control of ultracold polar molecules. Such systems of molecules promise the creation of long-lived, highly dipolar quantum gases with applications spanning the fields of quantum state controlled chemistry, quantum information, quantum simulation, and precision measurement. However, the addition of vibrational and rotational degrees of freedom leads to molecular systems being significantly more complex than their widely used atomic counterparts. In this work we demonstrate full control of the quantum state down to the hyperfine level of an optically trapped sample of ultracold bosonic 87Rb133 Cs molecules, and exploit that control to begin an investigation into the collision processes which take place in an ultracold molecular gas. We create a sample of up to ∼ 4000 optically trapped molecules in their rovibronic and hyperfine ground state. We characterise the molecules by measuring their temperature, binding energy, and molecule-frame electric dipole moment. We perform spectroscopy of the first rotationally excited state with hyperfine state resolution using microwaves to determine accurate values of rotational and hyperfine coupling constants. We use coherent π pulses to perform complete transfer population between selected hyperfine levels of the ground, first-excited, and second-excited rotational states. We investigate the effect of the off-resonant light of our optical dipole trap on the rotational and hyperfine structure of the molecules. Through a combination of high-resolution microwave spectroscopy and parametric heating measurements, we characterise the polarisability of the 87Rb133Cs molecule. We demonstrate that coupling between neighbouring hyperfine states manifests in rich structure with many avoided crossings in any rotational state other than the ground state. This coupling may be tuned by rotating the polarisation of the linearly polarised trapping light. Finally, we study the lifetime of polar bosonic 87Rb133Cs molecules in our 3D optical dipole trap. We examine the lifetime of the molecules as a function of dipole trap intensity, magnetic field, and hyperfine and rotational state. Despite the chemical stability of the 87Rb133 Cs molecule, we observe lifetimes of ∼1 s corresponding to 2-body decay rates close to the universal limit.